King cobra peptide OH-CATH30 as a potential candidate drug through clinic drug-resistant isolates.
King cobra peptide OH-CATH30 as a potential candidate drug through clinic drug-resistant isolates.
复制标题
通过临床耐药分离株将眼镜王蛇肽OH-CATH30作为潜在的候选药物。
DOI:
10.24272/j.issn.2095-8137.2018.025
复制
发表时间:
2018-03-18
影响因子:
4.9
通讯作者:
Zhang Y
中科院分区:
文献类型:
--
作者:
Zhao F;Lan XQ;Du Y;Chen PY;Zhao J;Zhao F;Lee WH;Zhang Y
Cationic antimicrobial peptides (AMPs) are considered as important candidate therapeutic agents, which exert potent microbicidal properties against bacteria, fungi and some viruses. Based on our previous findings king cobra cathelicidin (OH-CATH) is a 34-amino acid peptide that exerts strong antibacterial and weak hemolytic activity. The aim of this research is to evaluate the efficacy of both OH-CATH30 and its analog D-OH-CATH30 against clinical isolates comparing with routinely utilized antibiotics in vitro. In this study, 584 clinical isolates were tested (spanning 2013–2016) and the efficacy of the candidate peptides and antibiotics were determined by a broth microdilution method according to the CLSI guidelines. Among the 584 clinical isolates, 85% were susceptible to OH-CATH30 and its analogs. Both L- and D-OH-CATH30 showed higher efficacy against (toward) Gram-positive bacteria and stronger antibacterial activity against nearly all Gram-negative bacteria tested compare with antibiotics. The highest bactericidal activity was detected against Acinetobacter spp., including multi-drug-resistant Acinetobacter baumannii (MRAB) and methicillin-resistant Staphylococcus aureus (MRSA). The overall efficacy of OH-CATH30 and its analogs was higher than that of the 9 routinely used antibiotics. OH-CATH30 is a promising candidate drug for the treatment of a wide variety of bacterial infections which are resistant to many routinely used antimicrobial agents.
登录
查看更多内容
DOI:
10.1126/science.1176667
发表时间:
2009-08-28
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Fischbach MA;Walsh CT
通讯作者:
Walsh CT
影响因子:
4.4
作者:
Yang, Xinwang;Lee, Wen-Hui;Zhang, Yun
通讯作者:
Zhang, Yun
影响因子:
4.8
作者:
Johansson, J;Gudmundsson, GH;Agerberth, B
通讯作者:
Agerberth, B
影响因子:
5.5
作者:
PARK, E;QUINN, MR;SCHULLERLEVIS, G
通讯作者:
SCHULLERLEVIS, G
影响因子:
7
作者:
Tashima, Alexandre K.;Zelanis, Andre;Serrano, Solange M. T.
通讯作者:
Serrano, Solange M. T.